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Angela Bustamante - Academia.edu
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Views</span></p><p class="data"><span class="js-profile-view-count"></span></p></div></span></div><div class="ri-section"><div class="ri-section-header"><span>Interests</span></div><div class="ri-tags-container"><a data-click-track="profile-user-info-expand-research-interests" data-has-card-for-ri-list="44194127" href="https://www.academia.edu/Documents/in/Neurochemistry"><div id="js-react-on-rails-context" style="display:none" data-rails-context="{"inMailer":false,"i18nLocale":"en","i18nDefaultLocale":"en","href":"https://independent.academia.edu/AngelaBustamante2","location":"/AngelaBustamante2","scheme":"https","host":"independent.academia.edu","port":null,"pathname":"/AngelaBustamante2","search":null,"httpAcceptLanguage":null,"serverSide":false}"></div> <div class="js-react-on-rails-component" style="display:none" data-component-name="Pill" data-props="{"color":"gray","children":["Neurochemistry"]}" data-trace="false" data-dom-id="Pill-react-component-216cce76-918c-4110-8296-16a3e42e33f4"></div> <div id="Pill-react-component-216cce76-918c-4110-8296-16a3e42e33f4"></div> </a><a data-click-track="profile-user-info-expand-research-interests" data-has-card-for-ri-list="44194127" href="https://www.academia.edu/Documents/in/Vascular_dementia"><div class="js-react-on-rails-component" style="display:none" data-component-name="Pill" data-props="{"color":"gray","children":["Vascular dementia"]}" data-trace="false" data-dom-id="Pill-react-component-f241ed3c-f0f6-44ee-aae8-15eecb2d39cc"></div> <div id="Pill-react-component-f241ed3c-f0f6-44ee-aae8-15eecb2d39cc"></div> </a><a data-click-track="profile-user-info-expand-research-interests" data-has-card-for-ri-list="44194127" href="https://www.academia.edu/Documents/in/Functional_Connectivity"><div class="js-react-on-rails-component" style="display:none" data-component-name="Pill" data-props="{"color":"gray","children":["Functional Connectivity"]}" data-trace="false" data-dom-id="Pill-react-component-61180bd8-51c1-481c-a1fb-fa691299e52e"></div> <div id="Pill-react-component-61180bd8-51c1-481c-a1fb-fa691299e52e"></div> </a><a data-click-track="profile-user-info-expand-research-interests" data-has-card-for-ri-list="44194127" href="https://www.academia.edu/Documents/in/Movement_disorders"><div class="js-react-on-rails-component" style="display:none" data-component-name="Pill" data-props="{"color":"gray","children":["Movement disorders"]}" data-trace="false" data-dom-id="Pill-react-component-fa25076a-7c79-4b65-9601-d90452f143cf"></div> <div id="Pill-react-component-fa25076a-7c79-4b65-9601-d90452f143cf"></div> </a><a data-click-track="profile-user-info-expand-research-interests" data-has-card-for-ri-list="44194127" href="https://www.academia.edu/Documents/in/Movement"><div class="js-react-on-rails-component" style="display:none" data-component-name="Pill" data-props="{"color":"gray","children":["Movement"]}" data-trace="false" data-dom-id="Pill-react-component-eafd3160-3638-4717-8b8d-1b04f9f4b89a"></div> <div id="Pill-react-component-eafd3160-3638-4717-8b8d-1b04f9f4b89a"></div> </a></div></div></div></div><div class="right-panel-container"><div class="user-content-wrapper"><div class="uploads-container" id="social-redesign-work-container"><div class="upload-header"><h2 class="ds2-5-heading-sans-serif-xs">Uploads</h2></div><div class="documents-container backbone-social-profile-documents" style="width: 100%;"><div class="u-taCenter"></div><div class="profile--tab_content_container js-tab-pane tab-pane active" id="all"><div class="profile--tab_heading_container js-section-heading" data-section="Papers" id="Papers"><h3 class="profile--tab_heading_container">Papers by Angela Bustamante</h3></div><div class="js-work-strip profile--work_container" data-work-id="53155562"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155562/Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming"><img alt="Research paper thumbnail of Long-term survivors of murine sepsis are predisposed to enhanced LPS-induced lung injury and pro-inflammatory immune reprogramming" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155562/Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming">Long-term survivors of murine sepsis are predisposed to enhanced LPS-induced lung injury and pro-inflammatory immune reprogramming</a></div><div class="wp-workCard_item"><span>American Journal of Physiology-Lung Cellular and Molecular Physiology</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary complications. In order to prevent and treat these complications, biomarkers and molecular mediators must be identified. Persistent immune reprogramming in the form of immunoparalysis and impaired host defense is proposed to mediate late pulmonary complications after sepsis, particularly new pulmonary infections. However, immune reprogramming may also involve enhanced/primed responses to secondary stimuli, although their contribution to long-term sepsis complications remains understudied. We hypothesize that enhanced/primed immune responses in the lungs of sepsis survivors are associated with late pulmonary complications. To this end, we developed a murine sepsis model using cecal ligation and puncture (CLP) followed 3 weeks later by administration of intranasal lipopolysaccharide to induce inflammatory lung injury. Mice surviving sepsis exhibit enhanced lung injury with increased alveol...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155562"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155562"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155562; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155562]").text(description); $(".js-view-count[data-work-id=53155562]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155562; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155562']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155562, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=53155562]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155562,"title":"Long-term survivors of murine sepsis are predisposed to enhanced LPS-induced lung injury and pro-inflammatory immune reprogramming","translated_title":"","metadata":{"abstract":"Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary complications. In order to prevent and treat these complications, biomarkers and molecular mediators must be identified. Persistent immune reprogramming in the form of immunoparalysis and impaired host defense is proposed to mediate late pulmonary complications after sepsis, particularly new pulmonary infections. However, immune reprogramming may also involve enhanced/primed responses to secondary stimuli, although their contribution to long-term sepsis complications remains understudied. We hypothesize that enhanced/primed immune responses in the lungs of sepsis survivors are associated with late pulmonary complications. To this end, we developed a murine sepsis model using cecal ligation and puncture (CLP) followed 3 weeks later by administration of intranasal lipopolysaccharide to induce inflammatory lung injury. Mice surviving sepsis exhibit enhanced lung injury with increased alveol...","publisher":"American Physiological Society","publication_name":"American Journal of Physiology-Lung Cellular and Molecular Physiology"},"translated_abstract":"Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary complications. In order to prevent and treat these complications, biomarkers and molecular mediators must be identified. Persistent immune reprogramming in the form of immunoparalysis and impaired host defense is proposed to mediate late pulmonary complications after sepsis, particularly new pulmonary infections. However, immune reprogramming may also involve enhanced/primed responses to secondary stimuli, although their contribution to long-term sepsis complications remains understudied. We hypothesize that enhanced/primed immune responses in the lungs of sepsis survivors are associated with late pulmonary complications. To this end, we developed a murine sepsis model using cecal ligation and puncture (CLP) followed 3 weeks later by administration of intranasal lipopolysaccharide to induce inflammatory lung injury. Mice surviving sepsis exhibit enhanced lung injury with increased alveol...","internal_url":"https://www.academia.edu/53155562/Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming","translated_internal_url":"","created_at":"2021-09-21T13:01:30.841-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[],"research_interests":[{"id":167,"name":"Physiology","url":"https://www.academia.edu/Documents/in/Physiology"},{"id":186234,"name":"Medical Physiology","url":"https://www.academia.edu/Documents/in/Medical_Physiology"}],"urls":[{"id":11426416,"url":"https://journals.physiology.org/doi/pdf/10.1152/ajplung.00123.2021"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155561"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155561/Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood"><img alt="Research paper thumbnail of Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155561/Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood">Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and lik...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in DNA methylation (DNAm) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded.ResultsSelf-reported childhood FEH was nominally associated with right hemisphere hippocampus (b=10.4, p=0.005), left hemisphere amygdala (b=5.3, p=0.009), and right hemisphere amygdala (b=5.8, p=0.016) volumes. Childhood FEH was also nominally associated with 49 DNAm MEs (prange=3×10−6 to 0.047). After limiting analyses to probes correlated between saliva and brain, saliva-derived DNAm MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155561"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155561"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155561; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155561]").text(description); $(".js-view-count[data-work-id=53155561]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155561; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155561']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155561, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=53155561]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155561,"title":"Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood","translated_title":"","metadata":{"abstract":"BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in DNA methylation (DNAm) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded.ResultsSelf-reported childhood FEH was nominally associated with right hemisphere hippocampus (b=10.4, p=0.005), left hemisphere amygdala (b=5.3, p=0.009), and right hemisphere amygdala (b=5.8, p=0.016) volumes. Childhood FEH was also nominally associated with 49 DNAm MEs (prange=3×10−6 to 0.047). After limiting analyses to probes correlated between saliva and brain, saliva-derived DNAm MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect...","publisher":"Cold Spring Harbor Laboratory"},"translated_abstract":"BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in DNA methylation (DNAm) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded.ResultsSelf-reported childhood FEH was nominally associated with right hemisphere hippocampus (b=10.4, p=0.005), left hemisphere amygdala (b=5.3, p=0.009), and right hemisphere amygdala (b=5.8, p=0.016) volumes. Childhood FEH was also nominally associated with 49 DNAm MEs (prange=3×10−6 to 0.047). After limiting analyses to probes correlated between saliva and brain, saliva-derived DNAm MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect...","internal_url":"https://www.academia.edu/53155561/Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood","translated_internal_url":"","created_at":"2021-09-21T13:01:30.654-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[],"research_interests":[],"urls":[{"id":11426415,"url":"https://syndication.highwire.org/content/doi/10.1101/2020.10.26.355347"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155559"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155559/Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes"><img alt="Research paper thumbnail of Molecular genetic overlap between posttraumatic stress disorder and sleep phenotypes" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155559/Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes">Molecular genetic overlap between posttraumatic stress disorder and sleep phenotypes</a></div><div class="wp-workCard_item"><span>Sleep</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttrauma...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttraumatic stress disorder (PTSD), with these bidirectional relationships well established in the literature. While both sleep phenotypes and PTSD are moderately heritable, there has been a paucity of investigation into potential genetic overlap between sleep and PTSD. Here, we estimate genetic correlations between multiple sleep phenotypes (including insomnia symptoms, sleep duration, daytime sleepiness, and chronotype) and PTSD, using results from the largest genome-wide association study (GWAS) to date of PTSD, as well as publicly available GWAS results for sleep phenotypes within UK Biobank data (23 variations, encompassing four main phenotypes). Methods Genetic correlations were estimated utilizing linkage disequilibrium score regression (LDSC), an approach that uses GWAS summary statistics to compute genetic correlations across traits, and Mendelian randomization (MR) analyses were conduc...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155559"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155559"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155559; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155559]").text(description); $(".js-view-count[data-work-id=53155559]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155559; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155559']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155559, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=53155559]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155559,"title":"Molecular genetic overlap between posttraumatic stress disorder and sleep phenotypes","translated_title":"","metadata":{"abstract":"Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttraumatic stress disorder (PTSD), with these bidirectional relationships well established in the literature. While both sleep phenotypes and PTSD are moderately heritable, there has been a paucity of investigation into potential genetic overlap between sleep and PTSD. Here, we estimate genetic correlations between multiple sleep phenotypes (including insomnia symptoms, sleep duration, daytime sleepiness, and chronotype) and PTSD, using results from the largest genome-wide association study (GWAS) to date of PTSD, as well as publicly available GWAS results for sleep phenotypes within UK Biobank data (23 variations, encompassing four main phenotypes). Methods Genetic correlations were estimated utilizing linkage disequilibrium score regression (LDSC), an approach that uses GWAS summary statistics to compute genetic correlations across traits, and Mendelian randomization (MR) analyses were conduc...","publisher":"Oxford University Press (OUP)","publication_name":"Sleep"},"translated_abstract":"Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttraumatic stress disorder (PTSD), with these bidirectional relationships well established in the literature. While both sleep phenotypes and PTSD are moderately heritable, there has been a paucity of investigation into potential genetic overlap between sleep and PTSD. Here, we estimate genetic correlations between multiple sleep phenotypes (including insomnia symptoms, sleep duration, daytime sleepiness, and chronotype) and PTSD, using results from the largest genome-wide association study (GWAS) to date of PTSD, as well as publicly available GWAS results for sleep phenotypes within UK Biobank data (23 variations, encompassing four main phenotypes). Methods Genetic correlations were estimated utilizing linkage disequilibrium score regression (LDSC), an approach that uses GWAS summary statistics to compute genetic correlations across traits, and Mendelian randomization (MR) analyses were conduc...","internal_url":"https://www.academia.edu/53155559/Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes","translated_internal_url":"","created_at":"2021-09-21T13:01:30.462-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[],"research_interests":[{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences"},{"id":133324,"name":"Sleep","url":"https://www.academia.edu/Documents/in/Sleep"},{"id":2922956,"name":"Psychology and Cognitive Sciences","url":"https://www.academia.edu/Documents/in/Psychology_and_Cognitive_Sciences"},{"id":3763225,"name":"Medical and Health Sciences","url":"https://www.academia.edu/Documents/in/Medical_and_Health_Sciences"}],"urls":[{"id":11426414,"url":"http://academic.oup.com/sleep/advance-article-pdf/doi/10.1093/sleep/zsz257/31221055/zsz257.pdf"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155558"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155558/International_meta_analysis_of_PTSD_genome_wide_association_studies_identifies_sex_and_ancestry_specific_genetic_risk_loci"><img alt="Research paper thumbnail of International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci" class="work-thumbnail" src="https://attachments.academia-assets.com/70075877/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155558/International_meta_analysis_of_PTSD_genome_wide_association_studies_identifies_sex_and_ancestry_specific_genetic_risk_loci">International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci</a></div><div class="wp-workCard_item"><span>Nature Communications</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5–20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson’s disease gene involved in dopamine regulation, PARK2, is associated with PTSD. Finally, we demonstrate that polygenic risk for PTSD is significantly predictive of re-experiencing symptoms in the Million Veteran Program dataset, although specific loci did not replicate. These results demonstrate the role of genetic variation in the biology of risk for PTSD and highlight the necessity of conducting sex-stratified analyses and exp...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="d2f08e2ab12f2d71fec406719848e9a5" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075877,"asset_id":53155558,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075877/download_file?st=MTczMjc3NzAwMSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155558"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155558"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155558; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155558]").text(description); $(".js-view-count[data-work-id=53155558]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155558; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155558']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155558, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "d2f08e2ab12f2d71fec406719848e9a5" } } $('.js-work-strip[data-work-id=53155558]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155558,"title":"International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci","translated_title":"","metadata":{"abstract":"The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5–20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson’s disease gene involved in dopamine regulation, PARK2, is associated with PTSD. Finally, we demonstrate that polygenic risk for PTSD is significantly predictive of re-experiencing symptoms in the Million Veteran Program dataset, although specific loci did not replicate. These results demonstrate the role of genetic variation in the biology of risk for PTSD and highlight the necessity of conducting sex-stratified analyses and exp...","publisher":"Springer Science and Business Media LLC","publication_name":"Nature Communications"},"translated_abstract":"The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5–20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson’s disease gene involved in dopamine regulation, PARK2, is associated with PTSD. 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DNMT inhibitors alter DNA methylation globally in the brain and at individual neural plasticity-associated genes, but how DNMT inhibitors centrally influence lipopolysaccharide (LPS)-induced neuroinflammation is not known. We investigated whether the DMNT inhibitor, zebularine, would alter sickness behavior, DNA methylation of the Il-1β promoter and expression of inflammatory genes in hippocampus and microglia. Contrary to our hypothesis that zebularine may exaggerate LPS-induced sickness response and neuroinflammation, adult mice treated with an intracerebroventricular (ICV) injection of zebularine prior to LPS had surprisingly faster recovery of burrowing behavior compared to mice treated with LPS. Further, genes of inflammatory markers, epigenetic regulators, and the microglial sensory apparatus (i.e., the sensome) were differentially expressed by zebularine alone or in combination with LPS. Bisulfite pyrosequencing revealed that ICV zebularine led to decreased DNA methylation of two CpG sites near the Il-1β proximal promoter alone or in combination with LPS. Zebularine treated mice still exhibited decreased DNA methylation 48 h after treatment when LPS-induced sickness behavior as well as hippocampal and microglial gene expression were similar to control mice. 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The risk of PTSD fol...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Post-traumatic stress disorder (PTSD) is a common and debilitating disorder. The risk of PTSD following trauma is heritable, but robust common variants have yet to be identified by genome-wide association studies (GWAS). We have collected a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls. We first demonstrate significant genetic correlations across 60 PTSD cohorts to evaluate the comparability of these phenotypically heterogeneous studies. In this largest GWAS meta-analysis of PTSD to date we identify a total of 6 genome-wide significant loci, 4 in European and 2 in African-ancestry analyses. Follow-up analyses incorporated local ancestry and sex-specific effects, and functional studies. Along with other novel genes, a non-coding RNA (ncRNA) and a Parkinson&#39;s Disease gene, PARK2, were associated with PTSD. Consistent with previous reports, SNP-based heritability estimates for PTSD range between 10-20%. Despite a significant shared liability between PTSD...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="717cc0ae1ff05e10f9d91e3a25efaeaf" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075906,"asset_id":53155554,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075906/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155554"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155554"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155554; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155554]").text(description); $(".js-view-count[data-work-id=53155554]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155554; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155554']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155554, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "717cc0ae1ff05e10f9d91e3a25efaeaf" } } $('.js-work-strip[data-work-id=53155554]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155554,"title":"Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways","translated_title":"","metadata":{"abstract":"Post-traumatic stress disorder (PTSD) is a common and debilitating disorder. 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Epigenetic Modifications of Stress-Relevant Genes as Peripheral Biomarkers of Treatment-Resistant Depression","translated_title":"","metadata":{"publisher":"Elsevier BV","publication_name":"Biological Psychiatry"},"translated_abstract":null,"internal_url":"https://www.academia.edu/53155553/501_Epigenetic_Modifications_of_Stress_Relevant_Genes_as_Peripheral_Biomarkers_of_Treatment_Resistant_Depression","translated_internal_url":"","created_at":"2021-09-21T13:01:29.403-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"501_Epigenetic_Modifications_of_Stress_Relevant_Genes_as_Peripheral_Biomarkers_of_Treatment_Resistant_Depression","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[],"research_interests":[{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences"},{"id":49600,"name":"Biological Psychiatry","url":"https://www.academia.edu/Documents/in/Biological_Psychiatry"},{"id":2922956,"name":"Psychology and Cognitive Sciences","url":"https://www.academia.edu/Documents/in/Psychology_and_Cognitive_Sciences"},{"id":3763225,"name":"Medical and Health Sciences","url":"https://www.academia.edu/Documents/in/Medical_and_Health_Sciences"}],"urls":[{"id":11426408,"url":"http://api.elsevier.com/content/article/PII:S0006322317312313?httpAccept=text/plain"}]}, dispatcherData: dispatcherData }); 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155550"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155550/Glucocorticoid_Receptor_DNA_methylation_Childhood_Maltreatment_and_Major_Depression"><img alt="Research paper thumbnail of Glucocorticoid Receptor DNA methylation, Childhood Maltreatment and Major Depression" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155550/Glucocorticoid_Receptor_DNA_methylation_Childhood_Maltreatment_and_Major_Depression">Glucocorticoid Receptor DNA methylation, Childhood Maltreatment and Major Depression</a></div><div class="wp-workCard_item"><span>Journal of Affective Disorders</span><span>, 2016</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155550"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155550"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155550; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155549"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155549/Corrigendum_DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression"><img alt="Research paper thumbnail of Corrigendum: DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression" class="work-thumbnail" src="https://attachments.academia-assets.com/70075905/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155549/Corrigendum_DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression">Corrigendum: DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression</a></div><div class="wp-workCard_item"><span>Nature communications</span><span>, Jan 3, 2016</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2283a7350c15be0582884ac1f3f8f1af" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075905,"asset_id":53155549,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075905/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155549"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155549"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155549; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155548"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155548/DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression"><img alt="Research paper thumbnail of DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression" class="work-thumbnail" src="https://attachments.academia-assets.com/70075910/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155548/DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression">DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression</a></div><div class="wp-workCard_item"><span>Nature communications</span><span>, Jan 3, 2015</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">DICER1 is an enzyme that generates mature microRNAs (miRNAs), which regulate gene expression post...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">DICER1 is an enzyme that generates mature microRNAs (miRNAs), which regulate gene expression post-transcriptionally in brain and other tissues and is involved in synaptic maturation and plasticity. Here, through genome-wide differential gene expression survey of post-traumatic stress disorder (PTSD) with comorbid depression (PTSD&Dep), we find that blood DICER1 expression is significantly reduced in cases versus controls, and replicate this in two independent cohorts. Our follow-up studies find that lower blood DICER1 expression is significantly associated with increased amygdala activation to fearful stimuli, a neural correlate for PTSD. Additionally, a genetic variant in the 3&#39; un-translated region of DICER1, rs10144436, is significantly associated with DICER1 expression and with PTSD&Dep, and the latter is replicated in an independent cohort. Furthermore, genome-wide differential expression survey of miRNAs in blood in PTSD&Dep reveals miRNAs to be significantly downregulated...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="1a05b0b8af27052202022aa6ffeffdcf" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075910,"asset_id":53155548,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075910/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155548"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155548"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155548; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155548]").text(description); $(".js-view-count[data-work-id=53155548]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155548; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155548']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155548, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "1a05b0b8af27052202022aa6ffeffdcf" } } $('.js-work-strip[data-work-id=53155548]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155548,"title":"DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression","translated_title":"","metadata":{"abstract":"DICER1 is an enzyme that generates mature microRNAs (miRNAs), which regulate gene expression post-transcriptionally in brain and other tissues and is involved in synaptic maturation and plasticity. Here, through genome-wide differential gene expression survey of post-traumatic stress disorder (PTSD) with comorbid depression (PTSD\u0026Dep), we find that blood DICER1 expression is significantly reduced in cases versus controls, and replicate this in two independent cohorts. Our follow-up studies find that lower blood DICER1 expression is significantly associated with increased amygdala activation to fearful stimuli, a neural correlate for PTSD. Additionally, a genetic variant in the 3\u0026#39; un-translated region of DICER1, rs10144436, is significantly associated with DICER1 expression and with PTSD\u0026Dep, and the latter is replicated in an independent cohort. Furthermore, genome-wide differential expression survey of miRNAs in blood in PTSD\u0026Dep reveals miRNAs to be significantly downregulated...","publication_date":{"day":3,"month":1,"year":2015,"errors":{}},"publication_name":"Nature communications"},"translated_abstract":"DICER1 is an enzyme that generates mature microRNAs (miRNAs), which regulate gene expression post-transcriptionally in brain and other tissues and is involved in synaptic maturation and plasticity. Here, through genome-wide differential gene expression survey of post-traumatic stress disorder (PTSD) with comorbid depression (PTSD\u0026Dep), we find that blood DICER1 expression is significantly reduced in cases versus controls, and replicate this in two independent cohorts. Our follow-up studies find that lower blood DICER1 expression is significantly associated with increased amygdala activation to fearful stimuli, a neural correlate for PTSD. Additionally, a genetic variant in the 3\u0026#39; un-translated region of DICER1, rs10144436, is significantly associated with DICER1 expression and with PTSD\u0026Dep, and the latter is replicated in an independent cohort. Furthermore, genome-wide differential expression survey of miRNAs in blood in PTSD\u0026Dep reveals miRNAs to be significantly downregulated...","internal_url":"https://www.academia.edu/53155548/DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression","translated_internal_url":"","created_at":"2021-09-21T13:01:28.885-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":70075910,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/70075910/thumbnails/1.jpg","file_name":"4686835.pdf","download_url":"https://www.academia.edu/attachments/70075910/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"DICER1_and_microRNA_regulation_in_post_t.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/70075910/4686835-libre.pdf?1632254707=\u0026response-content-disposition=attachment%3B+filename%3DDICER1_and_microRNA_regulation_in_post_t.pdf\u0026Expires=1732780602\u0026Signature=GGSAP2eCmziDzFvoiU7sBZ3rq3zdBBybH9ZClu-vV-5-jT5L~CDsZcahQiURNHkznl17YsFcCois-LtRZ-roOq1PgjFH5~d4SYOqoXAMUH0hqJ~txQETo4irmiREYqzVMWYKtsKUAi-7jGsCsCd4BOoaYt88xRZswbCNCKNVPKmBVPtiA~OeVCKlgRBKKnEQ2~fpiLESDGKC3BpBLrS59i9Tbi9TH4r20Qt8axqRgP4aeGN8PMLilt8MRXQld8pmIQfeK-0BToxPlUjNtUAYzJ-NUoeztrL2ycPyc7zrrVsU67-Zmd-OTB-IeizSaaSbjBCj7~4l0VI34lpLmBkUMw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression","translated_slug":"","page_count":13,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[{"id":70075910,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/70075910/thumbnails/1.jpg","file_name":"4686835.pdf","download_url":"https://www.academia.edu/attachments/70075910/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"DICER1_and_microRNA_regulation_in_post_t.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/70075910/4686835-libre.pdf?1632254707=\u0026response-content-disposition=attachment%3B+filename%3DDICER1_and_microRNA_regulation_in_post_t.pdf\u0026Expires=1732780602\u0026Signature=GGSAP2eCmziDzFvoiU7sBZ3rq3zdBBybH9ZClu-vV-5-jT5L~CDsZcahQiURNHkznl17YsFcCois-LtRZ-roOq1PgjFH5~d4SYOqoXAMUH0hqJ~txQETo4irmiREYqzVMWYKtsKUAi-7jGsCsCd4BOoaYt88xRZswbCNCKNVPKmBVPtiA~OeVCKlgRBKKnEQ2~fpiLESDGKC3BpBLrS59i9Tbi9TH4r20Qt8axqRgP4aeGN8PMLilt8MRXQld8pmIQfeK-0BToxPlUjNtUAYzJ-NUoeztrL2ycPyc7zrrVsU67-Zmd-OTB-IeizSaaSbjBCj7~4l0VI34lpLmBkUMw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":3217,"name":"Depression","url":"https://www.academia.edu/Documents/in/Depression"},{"id":3931,"name":"Fear","url":"https://www.academia.edu/Documents/in/Fear"},{"id":28235,"name":"Multidisciplinary","url":"https://www.academia.edu/Documents/in/Multidisciplinary"},{"id":159962,"name":"Amygdala","url":"https://www.academia.edu/Documents/in/Amygdala"},{"id":295854,"name":"microRNAs","url":"https://www.academia.edu/Documents/in/microRNAs"},{"id":1267800,"name":"Nature Communications","url":"https://www.academia.edu/Documents/in/Nature_Communications"},{"id":1819400,"name":"Cohort Studies","url":"https://www.academia.edu/Documents/in/Cohort_Studies"},{"id":2039739,"name":"Down-Regulation","url":"https://www.academia.edu/Documents/in/Down-Regulation"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155547"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155547/Epidemiology_Epigenetics_and_Psychopathology"><img alt="Research paper thumbnail of Epidemiology, Epigenetics, and Psychopathology" class="work-thumbnail" src="https://attachments.academia-assets.com/70075907/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155547/Epidemiology_Epigenetics_and_Psychopathology">Epidemiology, Epigenetics, and Psychopathology</a></div><div class="wp-workCard_item"><span>Medical Epigenetics</span><span>, 2014</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2f571daa5413810bec8e9ceaf0478227" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075907,"asset_id":53155547,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075907/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155547"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155547"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155547; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "2f571daa5413810bec8e9ceaf0478227" } } $('.js-work-strip[data-work-id=53155547]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155547,"title":"Epidemiology, Epigenetics, and Psychopathology","translated_title":"","metadata":{"publisher":"S. Karger AG","ai_title_tag":"Linking Epigenetics and Psychopathology: A Review","grobid_abstract":"The link between environmental exposure and onset of psychopathology has been well documented, yet the pathway is not fully understood. Epigenetic modifications are thought to play a role in the manifestation of disease as studies have shown that early environmental exposures can influence epigenetic variation in both humans and other animals. As a result, epigenetic epidemiology studies with a specific focus on psychopathology will play an important role in elucidating the pathway to disease onset. In order to gain a clear perspective of where this field currently stands, here we provide a brief review of important issues in epigenetic epidemiology studies of psychopathology, including causal inference, common study designs, challenges faced with current study designs, and the importance of a life course perspective. We provide the reader with relevant examples of studies when appropriate, with a particular focus on studies that have examined the epigenetic modification of DNA methylation. Implications for future research are also discussed.","publication_date":{"day":null,"month":null,"year":2014,"errors":{}},"publication_name":"Medical Epigenetics","grobid_abstract_attachment_id":70075907},"translated_abstract":null,"internal_url":"https://www.academia.edu/53155547/Epidemiology_Epigenetics_and_Psychopathology","translated_internal_url":"","created_at":"2021-09-21T13:01:28.777-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":70075907,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/70075907/thumbnails/1.jpg","file_name":"362762.pdf","download_url":"https://www.academia.edu/attachments/70075907/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Epidemiology_Epigenetics_and_Psychopatho.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/70075907/362762-libre.pdf?1632254710=\u0026response-content-disposition=attachment%3B+filename%3DEpidemiology_Epigenetics_and_Psychopatho.pdf\u0026Expires=1732780602\u0026Signature=dSMSMI8uxa~Lzn-ktp7wPtQEuTx71z2dO3oLpjBLlW2vnaAs0qIpy0RSYEolaYoeOxCDIAyfkyYruyAlDYRq3lGRKSeIY-pB-wAkn8WZw0zdk1RFA1JvgseXR02NijD5gZZVNosaAc2WPNYh6pDVQQ~TvaWayWZ21FHQHXazJWHxVgwogf8p-xNRiTi6wf3ZRv5huHevCb~MI2XOmblS5B1grhJHEic3Qmvv7dVZa7wEgA3hBLc7L0CirIT7OUs1OaRHm0-E28EtTPFwVyMh-IuT6SP1cS8OtnPXyXhCFld2tmDyJBOf93sCwukJB6fcNpIHSnzPVN-3KkvK0sHSIQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Epidemiology_Epigenetics_and_Psychopathology","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[{"id":70075907,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/70075907/thumbnails/1.jpg","file_name":"362762.pdf","download_url":"https://www.academia.edu/attachments/70075907/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Epidemiology_Epigenetics_and_Psychopatho.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/70075907/362762-libre.pdf?1632254710=\u0026response-content-disposition=attachment%3B+filename%3DEpidemiology_Epigenetics_and_Psychopatho.pdf\u0026Expires=1732780602\u0026Signature=dSMSMI8uxa~Lzn-ktp7wPtQEuTx71z2dO3oLpjBLlW2vnaAs0qIpy0RSYEolaYoeOxCDIAyfkyYruyAlDYRq3lGRKSeIY-pB-wAkn8WZw0zdk1RFA1JvgseXR02NijD5gZZVNosaAc2WPNYh6pDVQQ~TvaWayWZ21FHQHXazJWHxVgwogf8p-xNRiTi6wf3ZRv5huHevCb~MI2XOmblS5B1grhJHEic3Qmvv7dVZa7wEgA3hBLc7L0CirIT7OUs1OaRHm0-E28EtTPFwVyMh-IuT6SP1cS8OtnPXyXhCFld2tmDyJBOf93sCwukJB6fcNpIHSnzPVN-3KkvK0sHSIQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155546"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155546/Epigenetics_Stress_and_Their_Potential_Impact_on_Brain_Network_Function_A_Focus_on_the_Schizophrenia_Diatheses"><img alt="Research paper thumbnail of Epigenetics, Stress, and Their Potential Impact on Brain Network Function: A Focus on the Schizophrenia Diatheses" class="work-thumbnail" src="https://attachments.academia-assets.com/70075930/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155546/Epigenetics_Stress_and_Their_Potential_Impact_on_Brain_Network_Function_A_Focus_on_the_Schizophrenia_Diatheses">Epigenetics, Stress, and Their Potential Impact on Brain Network Function: A Focus on the Schizophrenia Diatheses</a></div><div class="wp-workCard_item"><span>Frontiers in Psychiatry</span><span>, 2014</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="da8de4b7dd635637e8f557a0fb63424e" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075930,"asset_id":53155546,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075930/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155546"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155546"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155546; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155482"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155482/Childhood_maltreatment_is_associated_with_epigenetic_differences_in_hypothalamic_pituitary_adrenal_HPA_axis_genes_in_the_Detroit_Neighborhood_Health_Study"><img alt="Research paper thumbnail of Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155482/Childhood_maltreatment_is_associated_with_epigenetic_differences_in_hypothalamic_pituitary_adrenal_HPA_axis_genes_in_the_Detroit_Neighborhood_Health_Study">Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study</a></div><div class="wp-workCard_item"><span>Comprehensive Psychiatry</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155482"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155482"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155482; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="22605646"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/22605646/Childhood_maltreatment_is_associated_with_epigenetic_differences_in_hypothalamic_pituitary_adrenal_HPA_axis_genes_in_the_Detroit_Neighborhood_Health_Study"><img alt="Research paper thumbnail of Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/22605646/Childhood_maltreatment_is_associated_with_epigenetic_differences_in_hypothalamic_pituitary_adrenal_HPA_axis_genes_in_the_Detroit_Neighborhood_Health_Study">Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://illinois.academia.edu/DWildman">Derek Wildman</a> and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/AngelaBustamante2">Angela Bustamante</a></span></div><div class="wp-workCard_item"><span>Comprehensive Psychiatry</span><span>, 2013</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="22605646"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="22605646"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 22605646; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=22605646]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":22605646,"title":"Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study","translated_title":"","metadata":{"publication_date":{"day":null,"month":null,"year":2013,"errors":{}},"publication_name":"Comprehensive Psychiatry"},"translated_abstract":null,"internal_url":"https://www.academia.edu/22605646/Childhood_maltreatment_is_associated_with_epigenetic_differences_in_hypothalamic_pituitary_adrenal_HPA_axis_genes_in_the_Detroit_Neighborhood_Health_Study","translated_internal_url":"","created_at":"2016-02-29T09:10:15.336-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44163928,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[{"id":16307631,"work_id":22605646,"tagging_user_id":44163928,"tagged_user_id":null,"co_author_invite_id":254647,"email":"k***5@columbia.edu","display_order":0,"name":"Karestan Koenen","title":"Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study"},{"id":16307720,"work_id":22605646,"tagging_user_id":44163928,"tagged_user_id":53487504,"co_author_invite_id":674239,"email":"a***o@email.unc.edu","display_order":4194304,"name":"Allison Aiello","title":"Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study"},{"id":16307748,"work_id":22605646,"tagging_user_id":44163928,"tagged_user_id":null,"co_author_invite_id":1057349,"email":"s***a@bu.edu","display_order":6291456,"name":"Sandro Galea","title":"Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study"},{"id":16307878,"work_id":22605646,"tagging_user_id":44163928,"tagged_user_id":44194127,"co_author_invite_id":3755714,"email":"a***2@illinois.edu","display_order":7340032,"name":"Angela Bustamante","title":"Childhood maltreatment is associated with epigenetic differences in hypothalamic-pituitary-adrenal (HPA) axis genes in the Detroit Neighborhood Health Study"}],"downloadable_attachments":[],"slug":"Childhood_maltreatment_is_associated_with_epigenetic_differences_in_hypothalamic_pituitary_adrenal_HPA_axis_genes_in_the_Detroit_Neighborhood_Health_Study","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44163928,"first_name":"Derek","middle_initials":null,"last_name":"Wildman","page_name":"DWildman","domain_name":"illinois","created_at":"2016-02-29T09:09:40.545-08:00","display_name":"Derek Wildman","url":"https://illinois.academia.edu/DWildman","email":"dloyclNhc3gwZFAwT0NDUHhnUUlDbEt6NDNoSEEzOGpCM0QzcmUzWjduST0tLS84SnJOT0tBQWhVSC93eXJsQm5IM0E9PQ==--71ace2162daa8e07299388a7c743467e7ce9069f"},"attachments":[],"research_interests":[{"id":244814,"name":"Clinical Sciences","url":"https://www.academia.edu/Documents/in/Clinical_Sciences"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="4718380" id="papers"><div class="js-work-strip profile--work_container" data-work-id="53155562"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155562/Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming"><img alt="Research paper thumbnail of Long-term survivors of murine sepsis are predisposed to enhanced LPS-induced lung injury and pro-inflammatory immune reprogramming" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155562/Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming">Long-term survivors of murine sepsis are predisposed to enhanced LPS-induced lung injury and pro-inflammatory immune reprogramming</a></div><div class="wp-workCard_item"><span>American Journal of Physiology-Lung Cellular and Molecular Physiology</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary complications. In order to prevent and treat these complications, biomarkers and molecular mediators must be identified. Persistent immune reprogramming in the form of immunoparalysis and impaired host defense is proposed to mediate late pulmonary complications after sepsis, particularly new pulmonary infections. However, immune reprogramming may also involve enhanced/primed responses to secondary stimuli, although their contribution to long-term sepsis complications remains understudied. We hypothesize that enhanced/primed immune responses in the lungs of sepsis survivors are associated with late pulmonary complications. To this end, we developed a murine sepsis model using cecal ligation and puncture (CLP) followed 3 weeks later by administration of intranasal lipopolysaccharide to induce inflammatory lung injury. Mice surviving sepsis exhibit enhanced lung injury with increased alveol...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155562"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155562"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155562; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155562]").text(description); $(".js-view-count[data-work-id=53155562]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155562; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155562']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155562, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=53155562]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155562,"title":"Long-term survivors of murine sepsis are predisposed to enhanced LPS-induced lung injury and pro-inflammatory immune reprogramming","translated_title":"","metadata":{"abstract":"Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary complications. In order to prevent and treat these complications, biomarkers and molecular mediators must be identified. Persistent immune reprogramming in the form of immunoparalysis and impaired host defense is proposed to mediate late pulmonary complications after sepsis, particularly new pulmonary infections. However, immune reprogramming may also involve enhanced/primed responses to secondary stimuli, although their contribution to long-term sepsis complications remains understudied. We hypothesize that enhanced/primed immune responses in the lungs of sepsis survivors are associated with late pulmonary complications. To this end, we developed a murine sepsis model using cecal ligation and puncture (CLP) followed 3 weeks later by administration of intranasal lipopolysaccharide to induce inflammatory lung injury. Mice surviving sepsis exhibit enhanced lung injury with increased alveol...","publisher":"American Physiological Society","publication_name":"American Journal of Physiology-Lung Cellular and Molecular Physiology"},"translated_abstract":"Millions of people who survive sepsis each year are rehospitalized and die due to late pulmonary complications. In order to prevent and treat these complications, biomarkers and molecular mediators must be identified. Persistent immune reprogramming in the form of immunoparalysis and impaired host defense is proposed to mediate late pulmonary complications after sepsis, particularly new pulmonary infections. However, immune reprogramming may also involve enhanced/primed responses to secondary stimuli, although their contribution to long-term sepsis complications remains understudied. We hypothesize that enhanced/primed immune responses in the lungs of sepsis survivors are associated with late pulmonary complications. To this end, we developed a murine sepsis model using cecal ligation and puncture (CLP) followed 3 weeks later by administration of intranasal lipopolysaccharide to induce inflammatory lung injury. Mice surviving sepsis exhibit enhanced lung injury with increased alveol...","internal_url":"https://www.academia.edu/53155562/Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming","translated_internal_url":"","created_at":"2021-09-21T13:01:30.841-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Long_term_survivors_of_murine_sepsis_are_predisposed_to_enhanced_LPS_induced_lung_injury_and_pro_inflammatory_immune_reprogramming","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[],"research_interests":[{"id":167,"name":"Physiology","url":"https://www.academia.edu/Documents/in/Physiology"},{"id":186234,"name":"Medical Physiology","url":"https://www.academia.edu/Documents/in/Medical_Physiology"}],"urls":[{"id":11426416,"url":"https://journals.physiology.org/doi/pdf/10.1152/ajplung.00123.2021"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155561"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155561/Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood"><img alt="Research paper thumbnail of Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155561/Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood">Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and lik...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in DNA methylation (DNAm) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded.ResultsSelf-reported childhood FEH was nominally associated with right hemisphere hippocampus (b=10.4, p=0.005), left hemisphere amygdala (b=5.3, p=0.009), and right hemisphere amygdala (b=5.8, p=0.016) volumes. Childhood FEH was also nominally associated with 49 DNAm MEs (prange=3×10−6 to 0.047). After limiting analyses to probes correlated between saliva and brain, saliva-derived DNAm MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155561"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155561"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155561; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155561]").text(description); $(".js-view-count[data-work-id=53155561]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155561; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155561']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155561, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=53155561]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155561,"title":"Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood","translated_title":"","metadata":{"abstract":"BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in DNA methylation (DNAm) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded.ResultsSelf-reported childhood FEH was nominally associated with right hemisphere hippocampus (b=10.4, p=0.005), left hemisphere amygdala (b=5.3, p=0.009), and right hemisphere amygdala (b=5.8, p=0.016) volumes. Childhood FEH was also nominally associated with 49 DNAm MEs (prange=3×10−6 to 0.047). After limiting analyses to probes correlated between saliva and brain, saliva-derived DNAm MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect...","publisher":"Cold Spring Harbor Laboratory"},"translated_abstract":"BackgroundPoor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in DNA methylation (DNAm) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded.ResultsSelf-reported childhood FEH was nominally associated with right hemisphere hippocampus (b=10.4, p=0.005), left hemisphere amygdala (b=5.3, p=0.009), and right hemisphere amygdala (b=5.8, p=0.016) volumes. Childhood FEH was also nominally associated with 49 DNAm MEs (prange=3×10−6 to 0.047). After limiting analyses to probes correlated between saliva and brain, saliva-derived DNAm MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect...","internal_url":"https://www.academia.edu/53155561/Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood","translated_internal_url":"","created_at":"2021-09-21T13:01:30.654-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Associations_between_childhood_family_emotional_health_fronto_limbic_grey_matter_volume_and_saliva_5mC_in_young_adulthood","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[],"research_interests":[],"urls":[{"id":11426415,"url":"https://syndication.highwire.org/content/doi/10.1101/2020.10.26.355347"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155559"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155559/Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes"><img alt="Research paper thumbnail of Molecular genetic overlap between posttraumatic stress disorder and sleep phenotypes" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155559/Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes">Molecular genetic overlap between posttraumatic stress disorder and sleep phenotypes</a></div><div class="wp-workCard_item"><span>Sleep</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttrauma...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttraumatic stress disorder (PTSD), with these bidirectional relationships well established in the literature. While both sleep phenotypes and PTSD are moderately heritable, there has been a paucity of investigation into potential genetic overlap between sleep and PTSD. Here, we estimate genetic correlations between multiple sleep phenotypes (including insomnia symptoms, sleep duration, daytime sleepiness, and chronotype) and PTSD, using results from the largest genome-wide association study (GWAS) to date of PTSD, as well as publicly available GWAS results for sleep phenotypes within UK Biobank data (23 variations, encompassing four main phenotypes). Methods Genetic correlations were estimated utilizing linkage disequilibrium score regression (LDSC), an approach that uses GWAS summary statistics to compute genetic correlations across traits, and Mendelian randomization (MR) analyses were conduc...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155559"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155559"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155559; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155559]").text(description); $(".js-view-count[data-work-id=53155559]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155559; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155559']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155559, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=53155559]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155559,"title":"Molecular genetic overlap between posttraumatic stress disorder and sleep phenotypes","translated_title":"","metadata":{"abstract":"Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttraumatic stress disorder (PTSD), with these bidirectional relationships well established in the literature. While both sleep phenotypes and PTSD are moderately heritable, there has been a paucity of investigation into potential genetic overlap between sleep and PTSD. Here, we estimate genetic correlations between multiple sleep phenotypes (including insomnia symptoms, sleep duration, daytime sleepiness, and chronotype) and PTSD, using results from the largest genome-wide association study (GWAS) to date of PTSD, as well as publicly available GWAS results for sleep phenotypes within UK Biobank data (23 variations, encompassing four main phenotypes). Methods Genetic correlations were estimated utilizing linkage disequilibrium score regression (LDSC), an approach that uses GWAS summary statistics to compute genetic correlations across traits, and Mendelian randomization (MR) analyses were conduc...","publisher":"Oxford University Press (OUP)","publication_name":"Sleep"},"translated_abstract":"Study Objectives Sleep problems are common, serving as both a predictor and symptom of posttraumatic stress disorder (PTSD), with these bidirectional relationships well established in the literature. While both sleep phenotypes and PTSD are moderately heritable, there has been a paucity of investigation into potential genetic overlap between sleep and PTSD. Here, we estimate genetic correlations between multiple sleep phenotypes (including insomnia symptoms, sleep duration, daytime sleepiness, and chronotype) and PTSD, using results from the largest genome-wide association study (GWAS) to date of PTSD, as well as publicly available GWAS results for sleep phenotypes within UK Biobank data (23 variations, encompassing four main phenotypes). Methods Genetic correlations were estimated utilizing linkage disequilibrium score regression (LDSC), an approach that uses GWAS summary statistics to compute genetic correlations across traits, and Mendelian randomization (MR) analyses were conduc...","internal_url":"https://www.academia.edu/53155559/Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes","translated_internal_url":"","created_at":"2021-09-21T13:01:30.462-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Molecular_genetic_overlap_between_posttraumatic_stress_disorder_and_sleep_phenotypes","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[],"research_interests":[{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences"},{"id":133324,"name":"Sleep","url":"https://www.academia.edu/Documents/in/Sleep"},{"id":2922956,"name":"Psychology and Cognitive Sciences","url":"https://www.academia.edu/Documents/in/Psychology_and_Cognitive_Sciences"},{"id":3763225,"name":"Medical and Health Sciences","url":"https://www.academia.edu/Documents/in/Medical_and_Health_Sciences"}],"urls":[{"id":11426414,"url":"http://academic.oup.com/sleep/advance-article-pdf/doi/10.1093/sleep/zsz257/31221055/zsz257.pdf"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155558"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155558/International_meta_analysis_of_PTSD_genome_wide_association_studies_identifies_sex_and_ancestry_specific_genetic_risk_loci"><img alt="Research paper thumbnail of International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci" class="work-thumbnail" src="https://attachments.academia-assets.com/70075877/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155558/International_meta_analysis_of_PTSD_genome_wide_association_studies_identifies_sex_and_ancestry_specific_genetic_risk_loci">International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci</a></div><div class="wp-workCard_item"><span>Nature Communications</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5–20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson’s disease gene involved in dopamine regulation, PARK2, is associated with PTSD. Finally, we demonstrate that polygenic risk for PTSD is significantly predictive of re-experiencing symptoms in the Million Veteran Program dataset, although specific loci did not replicate. These results demonstrate the role of genetic variation in the biology of risk for PTSD and highlight the necessity of conducting sex-stratified analyses and exp...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="d2f08e2ab12f2d71fec406719848e9a5" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075877,"asset_id":53155558,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075877/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3NzAwMSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155558"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155558"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155558; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155558]").text(description); $(".js-view-count[data-work-id=53155558]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155558; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155558']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155558, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "d2f08e2ab12f2d71fec406719848e9a5" } } $('.js-work-strip[data-work-id=53155558]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155558,"title":"International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci","translated_title":"","metadata":{"abstract":"The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. 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These results demonstrate the role of genetic variation in the biology of risk for PTSD and highlight the necessity of conducting sex-stratified analyses and exp...","publisher":"Springer Science and Business Media LLC","publication_name":"Nature Communications"},"translated_abstract":"The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5–20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson’s disease gene involved in dopamine regulation, PARK2, is associated with PTSD. 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DNMT inhibitors alter DNA methylation globally in the brain and at individual neural plasticity-associated genes, but how DNMT inhibitors centrally influence lipopolysaccharide (LPS)-induced neuroinflammation is not known. We investigated whether the DMNT inhibitor, zebularine, would alter sickness behavior, DNA methylation of the Il-1β promoter and expression of inflammatory genes in hippocampus and microglia. Contrary to our hypothesis that zebularine may exaggerate LPS-induced sickness response and neuroinflammation, adult mice treated with an intracerebroventricular (ICV) injection of zebularine prior to LPS had surprisingly faster recovery of burrowing behavior compared to mice treated with LPS. Further, genes of inflammatory markers, epigenetic regulators, and the microglial sensory apparatus (i.e., the sensome) were differentially expressed by zebularine alone or in combination with LPS. Bisulfite pyrosequencing revealed that ICV zebularine led to decreased DNA methylation of two CpG sites near the Il-1β proximal promoter alone or in combination with LPS. Zebularine treated mice still exhibited decreased DNA methylation 48 h after treatment when LPS-induced sickness behavior as well as hippocampal and microglial gene expression were similar to control mice. 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The risk of PTSD fol...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Post-traumatic stress disorder (PTSD) is a common and debilitating disorder. The risk of PTSD following trauma is heritable, but robust common variants have yet to be identified by genome-wide association studies (GWAS). We have collected a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls. We first demonstrate significant genetic correlations across 60 PTSD cohorts to evaluate the comparability of these phenotypically heterogeneous studies. In this largest GWAS meta-analysis of PTSD to date we identify a total of 6 genome-wide significant loci, 4 in European and 2 in African-ancestry analyses. Follow-up analyses incorporated local ancestry and sex-specific effects, and functional studies. Along with other novel genes, a non-coding RNA (ncRNA) and a Parkinson&#39;s Disease gene, PARK2, were associated with PTSD. Consistent with previous reports, SNP-based heritability estimates for PTSD range between 10-20%. 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155548"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155548/DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression"><img alt="Research paper thumbnail of DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression" class="work-thumbnail" src="https://attachments.academia-assets.com/70075910/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155548/DICER1_and_microRNA_regulation_in_post_traumatic_stress_disorder_with_comorbid_depression">DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression</a></div><div class="wp-workCard_item"><span>Nature communications</span><span>, Jan 3, 2015</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">DICER1 is an enzyme that generates mature microRNAs (miRNAs), which regulate gene expression post...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">DICER1 is an enzyme that generates mature microRNAs (miRNAs), which regulate gene expression post-transcriptionally in brain and other tissues and is involved in synaptic maturation and plasticity. Here, through genome-wide differential gene expression survey of post-traumatic stress disorder (PTSD) with comorbid depression (PTSD&Dep), we find that blood DICER1 expression is significantly reduced in cases versus controls, and replicate this in two independent cohorts. Our follow-up studies find that lower blood DICER1 expression is significantly associated with increased amygdala activation to fearful stimuli, a neural correlate for PTSD. Additionally, a genetic variant in the 3&#39; un-translated region of DICER1, rs10144436, is significantly associated with DICER1 expression and with PTSD&Dep, and the latter is replicated in an independent cohort. Furthermore, genome-wide differential expression survey of miRNAs in blood in PTSD&Dep reveals miRNAs to be significantly downregulated...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="1a05b0b8af27052202022aa6ffeffdcf" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075910,"asset_id":53155548,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075910/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155548"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155548"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155548; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155548]").text(description); $(".js-view-count[data-work-id=53155548]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155548; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155548']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155548, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "1a05b0b8af27052202022aa6ffeffdcf" } } $('.js-work-strip[data-work-id=53155548]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155548,"title":"DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression","translated_title":"","metadata":{"abstract":"DICER1 is an enzyme that generates mature microRNAs (miRNAs), which regulate gene expression post-transcriptionally in brain and other tissues and is involved in synaptic maturation and plasticity. 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155547"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155547/Epidemiology_Epigenetics_and_Psychopathology"><img alt="Research paper thumbnail of Epidemiology, Epigenetics, and Psychopathology" class="work-thumbnail" src="https://attachments.academia-assets.com/70075907/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155547/Epidemiology_Epigenetics_and_Psychopathology">Epidemiology, Epigenetics, and Psychopathology</a></div><div class="wp-workCard_item"><span>Medical Epigenetics</span><span>, 2014</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2f571daa5413810bec8e9ceaf0478227" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075907,"asset_id":53155547,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075907/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155547"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155547"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155547; 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Karger AG","ai_title_tag":"Linking Epigenetics and Psychopathology: A Review","grobid_abstract":"The link between environmental exposure and onset of psychopathology has been well documented, yet the pathway is not fully understood. Epigenetic modifications are thought to play a role in the manifestation of disease as studies have shown that early environmental exposures can influence epigenetic variation in both humans and other animals. As a result, epigenetic epidemiology studies with a specific focus on psychopathology will play an important role in elucidating the pathway to disease onset. In order to gain a clear perspective of where this field currently stands, here we provide a brief review of important issues in epigenetic epidemiology studies of psychopathology, including causal inference, common study designs, challenges faced with current study designs, and the importance of a life course perspective. We provide the reader with relevant examples of studies when appropriate, with a particular focus on studies that have examined the epigenetic modification of DNA methylation. Implications for future research are also discussed.","publication_date":{"day":null,"month":null,"year":2014,"errors":{}},"publication_name":"Medical Epigenetics","grobid_abstract_attachment_id":70075907},"translated_abstract":null,"internal_url":"https://www.academia.edu/53155547/Epidemiology_Epigenetics_and_Psychopathology","translated_internal_url":"","created_at":"2021-09-21T13:01:28.777-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":44194127,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":70075907,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/70075907/thumbnails/1.jpg","file_name":"362762.pdf","download_url":"https://www.academia.edu/attachments/70075907/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Epidemiology_Epigenetics_and_Psychopatho.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/70075907/362762-libre.pdf?1632254710=\u0026response-content-disposition=attachment%3B+filename%3DEpidemiology_Epigenetics_and_Psychopatho.pdf\u0026Expires=1732780602\u0026Signature=dSMSMI8uxa~Lzn-ktp7wPtQEuTx71z2dO3oLpjBLlW2vnaAs0qIpy0RSYEolaYoeOxCDIAyfkyYruyAlDYRq3lGRKSeIY-pB-wAkn8WZw0zdk1RFA1JvgseXR02NijD5gZZVNosaAc2WPNYh6pDVQQ~TvaWayWZ21FHQHXazJWHxVgwogf8p-xNRiTi6wf3ZRv5huHevCb~MI2XOmblS5B1grhJHEic3Qmvv7dVZa7wEgA3hBLc7L0CirIT7OUs1OaRHm0-E28EtTPFwVyMh-IuT6SP1cS8OtnPXyXhCFld2tmDyJBOf93sCwukJB6fcNpIHSnzPVN-3KkvK0sHSIQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Epidemiology_Epigenetics_and_Psychopathology","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":44194127,"first_name":"Angela","middle_initials":null,"last_name":"Bustamante","page_name":"AngelaBustamante2","domain_name":"independent","created_at":"2016-02-29T18:54:51.552-08:00","display_name":"Angela Bustamante","url":"https://independent.academia.edu/AngelaBustamante2"},"attachments":[{"id":70075907,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/70075907/thumbnails/1.jpg","file_name":"362762.pdf","download_url":"https://www.academia.edu/attachments/70075907/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Epidemiology_Epigenetics_and_Psychopatho.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/70075907/362762-libre.pdf?1632254710=\u0026response-content-disposition=attachment%3B+filename%3DEpidemiology_Epigenetics_and_Psychopatho.pdf\u0026Expires=1732780602\u0026Signature=dSMSMI8uxa~Lzn-ktp7wPtQEuTx71z2dO3oLpjBLlW2vnaAs0qIpy0RSYEolaYoeOxCDIAyfkyYruyAlDYRq3lGRKSeIY-pB-wAkn8WZw0zdk1RFA1JvgseXR02NijD5gZZVNosaAc2WPNYh6pDVQQ~TvaWayWZ21FHQHXazJWHxVgwogf8p-xNRiTi6wf3ZRv5huHevCb~MI2XOmblS5B1grhJHEic3Qmvv7dVZa7wEgA3hBLc7L0CirIT7OUs1OaRHm0-E28EtTPFwVyMh-IuT6SP1cS8OtnPXyXhCFld2tmDyJBOf93sCwukJB6fcNpIHSnzPVN-3KkvK0sHSIQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="53155546"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/53155546/Epigenetics_Stress_and_Their_Potential_Impact_on_Brain_Network_Function_A_Focus_on_the_Schizophrenia_Diatheses"><img alt="Research paper thumbnail of Epigenetics, Stress, and Their Potential Impact on Brain Network Function: A Focus on the Schizophrenia Diatheses" class="work-thumbnail" src="https://attachments.academia-assets.com/70075930/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/53155546/Epigenetics_Stress_and_Their_Potential_Impact_on_Brain_Network_Function_A_Focus_on_the_Schizophrenia_Diatheses">Epigenetics, Stress, and Their Potential Impact on Brain Network Function: A Focus on the Schizophrenia Diatheses</a></div><div class="wp-workCard_item"><span>Frontiers in Psychiatry</span><span>, 2014</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="da8de4b7dd635637e8f557a0fb63424e" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":70075930,"asset_id":53155546,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/70075930/download_file?st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3NzAwMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="53155546"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="53155546"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 53155546; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=53155546]").text(description); $(".js-view-count[data-work-id=53155546]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 53155546; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='53155546']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 53155546, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "da8de4b7dd635637e8f557a0fb63424e" } } $('.js-work-strip[data-work-id=53155546]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":53155546,"title":"Epigenetics, Stress, and Their Potential Impact on Brain Network Function: A Focus on the Schizophrenia Diatheses","translated_title":"","metadata":{"publisher":"Frontiers Media SA","grobid_abstract":"The recent sociodevelopmental cognitive model of schizophrenia/psychosis is a highly influential and compelling compendium of research findings. Here, we present logical extensions to this model incorporating ideas drawn from epigenetic mediation of psychiatric disease, and the plausible effects of epigenetics on the emergence of brain network function and dysfunction in adolescence. We discuss how gene-environment interactions, effected by epigenetic mechanisms, might in particular mediate the stress response (itself heavily implicated in the emergence of schizophrenia). Next, we discuss the plausible relevance of this framework for adolescent genetic risk populations, a risk group characterized by vexing and difficult-to-explain heterogeneity. We then discuss how exploring relationships between epigenetics and brain network dysfunction (a strongly validated finding in risk populations) can enhance understanding of the relationship between stress, epigenetics, and functional neurobiology, and the relevance of this relationship for the eventual emergence of schizophrenia/psychosis. 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